Canonical Allele Identifier: CA1769101627
Gene: LPL HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.19954009C= , CM000670.2:g.19954009C= GRCh38
NC_000008.10:g.19811520C= , CM000670.1:g.19811520C= GRCh37
NC_000008.9:g.19855800C= NCBI36
NG_008855.1:g.19939C=
NG_008855.2:g.57293C=

Transcript Alleles

HGVS Amino-acid change
ENST00000650287.1:c.542-111C= MANE Select ENSP00000497642.1:n.542-111C=
ENST00000311322.8:c.542-111C= ENSP00000309757.6:n.542-111C=
ENST00000520959.5:c.314-111C= ENSP00000428496.1:n.314-111C=
NM_000237.2:c.542-111C= NP_000228.1:n.542-111C=
NM_000237.3:c.542-111C= MANE Select NP_000228.1:n.542-111C=
Search 100 bp 5'
Search 100 bp 3'